Clinical Research Associate - Site Monitoring Pro
-
Research/Development
Job Description & How to Apply Below
IQVIA is seeking a Clinical Research Associate to monitor study sites and ensure data integrity in line with the protocol, GCP, and sponsor requirements.
Responsibilities include site visits, recruitment tracking, protocol training, and maintaining TMF/ISF documentation while collaborating with the study team. A BA/BS in a scientific field and 2+ years on-site CRA experience are preferred.
Step into the Clinical Research Associate
- Site Monitoring Pro role at IQVIA in Ontario, CA, United States and grow with us.
We invite applications for the Clinical Research Associate
- Site Monitoring Pro position located in Ontario, CA, United States.
The following opening is for a Clinical Research Associate
- Site Monitoring Pro with IQVIA.
Our group is growing, and we are hiring a Clinical Research Associate
- Site Monitoring Pro in Ontario, CA, United States.
Position Requirements
10+ Years work experience(If this job is in fact in your jurisdiction, then you may be using a Proxy or VPN to access this site, and to progress further, you should change your connectivity to another mobile device or PC).
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